The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations
Patrick Frosk(University of Manitoba), Klaus Wrogemann, Nicole M. Roslin(McGill University Health Centre), Edward Nylen, Cheryl R. Greenberg(Children's Hospital Research Institute of Manitoba), Danielle Frappier(McGill University Health Centre), Alysa A.P. Tennese(University of Manitoba), Flavia Paula(Universidade de São Paulo), Ryan E. Lamont(Children's Hospital Research Institute of Manitoba), Mayana Zatz(Universidade de São Paulo), Cheryl Hirst(University of Manitoba), Takuya Fujiwara(Montreal General Hospital), Kenneth Morgan(University of London), M Zaik(University of Duisburg-Essen), Kate Bushby(Muscular Dystrophy UK), Volker Straub(Newcastle upon Tyne Hospitals NHS Foundation Trust)
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